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Mizuho OSI

Complete recall history across all FDA and CPSC categories — 6 total recalls

Mizuho OSI appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (6)

FDA medical device enforcement actions by Mizuho OSI

Date Product Reason Class
Jul 29, 2021 HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144 One batch of "regular" femoral hooks were incorrectly etched with the "classi... Class II
Feb 8, 2021 Mizuho CE IPX4, mode MOT-5602BW, 100-240, 50-60Hz, 400VA, REF 18-140-20 conta... There is a potential that hand control units may cause the tabletop to slide ... Class II
Oct 14, 2019 Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Labe... Due to the potential for fluid ingress into the Arm which could affect the de... Class II
Mar 28, 2017 216 Wilson Frame Pads, Model # 5319-37; Used with Radiolucent Wilson Frame... Mizuho has discovered that the 5319-37 Wilson Frame Pads have a design defici... Class II
Dec 14, 2015 Mizuho OSI Trios, Table Base; Voltage: 100-240V ~ 50/60 Hz Amps: 5,0-5.0A; ... Table Bases may have been assembled incorrectly, missing a retaining ring fro... Class II
Dec 17, 2012 Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table S... Possible instability of Orthopedic Table Top. If the epoxy bond fails, the a... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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